Catalog Number

AIH2FM3510S

Brand Name

IH2 Fixture SLA

Version/Model Number

AIH2FM3510S

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K153521

Product Code

DZE

Product Code Name

Implant, Endosseous, Root-Form

Public Device Record Key

c2301ca9-babd-4e5d-accb-4a18fd015311

Public Version Date

September 16, 2022

Public Version Number

2

DI Record Publish Date

July 02, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-